FDA UDI Not in Commercial Distribution 🇺🇸 United States

NA

DI: 07613327052176 · Model: 0250080122 · STRYKER CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
07613327052176
Version / Model
0250080122
Catalog Number
250-080-122
Company Name
STRYKER CORPORATION
Labeler DUNS
187502109
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
7
Public Version Date
2019-08-21
Public Version Status
Update
Public Device Record Key
3bd05cc6-643d-4ded-b5c9-9f2b2115cdcf
Distribution End Date
2019-02-15

Device Description

Bipolar Micro-Tip Forceps with Ring Handle

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
OCZ Endoscopic grasping/cutting instrument, non-powered

GMDN Terms

Code Name
35080 Rigid endoscopic tissue manipulation forceps, reusable

Identifiers

Type ID
Primary 07613327052176

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Diameter: 5.0 Millimeter
Length 33.0 Centimeter